Nickel Nanoparticles Immobilized over Mesoporous SBA-15 for Efficient Carbonylative Coupling Reactions Utilizing CO2: A Spotlight

Ecofriendly routes for the synthesis of carbamates and carbonylative coupling products such as benzyl formate derivatives are very demanding for both academia and industries. Foreseeing a sustainable green future, we systematically analyzed the synthesis history of both these chemicals, mentioning t...

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Published in:ACS applied materials & interfaces Vol. 13; no. 34; pp. 40157 - 40171
Main Authors: Chongdar, Sayantan, Bhattacharjee, Sudip, Azad, Shiyana, Samui, Surajit, Dutta, Saikat, Bal, Rajaram, Bhaumik, Asim
Format: Journal Article
Language:English
Published: American Chemical Society 01-09-2021
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Summary:Ecofriendly routes for the synthesis of carbamates and carbonylative coupling products such as benzyl formate derivatives are very demanding for both academia and industries. Foreseeing a sustainable green future, we systematically analyzed the synthesis history of both these chemicals, mentioning their pros and cons. As a step towards green chemistry, here we have optimized the reaction conditions for the synthesis of various benzyl formates from corresponding benzyl halides and carbamates from substituted anilines and alkyl halides catalyzed by Ni(0) nanoparticles (NPs) immobilized over amine-functionalized ordered mesoporous SBA-15 material in the presence of CO2 as C1 source. This spotlight on applications is aimed to provide a clear outlook to date regarding the gradual progress in the synthesis of both these aforementioned chemicals and finally addresses further efforts for overcoming the current challenges.
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ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.1c09942